ALCEDIAG/Sys2Diag, CNRS UMR 9005, Parc Euromédecine, Cap Delta, 1682 Rue de la Valsière, Montpellier, 34184, France.
Department of Emergency Psychiatry and Acute Care, University Hospital/INSERM U1061, 191 Av. du Doyen Gaston Giraud, Montpellier, 34295, France.
Transl Psychiatry. 2021 Apr 30;11(1):255. doi: 10.1038/s41398-021-01377-9.
Mental health issues, including major depressive disorder, which can lead to suicidal behavior, are considered by the World Health Organization as a major threat to global health. Alterations in neurotransmitter signaling, e.g., serotonin and glutamate, or inflammatory response have been linked to both MDD and suicide. Phosphodiesterase 8A (PDE8A) gene expression is significantly decreased in the temporal cortex of major depressive disorder (MDD) patients. PDE8A specifically hydrolyzes adenosine 3',5'-cyclic monophosphate (cAMP), which is a key second messenger involved in inflammation, cognition, and chronic antidepressant treatment. Moreover, alterations of RNA editing in PDE8A mRNA has been described in the brain of depressed suicide decedents. Here, we investigated PDE8A A-to-I RNA editing-related modifications in whole blood of depressed patients and suicide attempters compared to age-matched and sex-matched healthy controls. We report significant alterations of RNA editing of PDE8A in the blood of depressed patients and suicide attempters with major depression, for which the suicide attempt took place during the last month before sample collection. The reported RNA editing modifications in whole blood were similar to the changes observed in the brain of suicide decedents. Furthermore, analysis and combinations of different edited isoforms allowed us to discriminate between suicide attempters and control groups. Altogether, our results identify PDE8A as an immune response-related marker whose RNA editing modifications translate from brain to blood, suggesting that monitoring RNA editing in PDE8A in blood samples could help to evaluate depressive state and suicide risk.
心理健康问题,包括可能导致自杀行为的重度抑郁症,被世界卫生组织视为对全球健康的主要威胁。神经递质信号转导的改变,如血清素和谷氨酸,或炎症反应,与 MDD 和自杀都有关联。在重度抑郁症(MDD)患者的颞叶皮层中,磷酸二酯酶 8A(PDE8A)基因的表达显著降低。PDE8A 专门水解环磷酸腺苷(cAMP),cAMP 是一种涉及炎症、认知和慢性抗抑郁治疗的关键第二信使。此外,在抑郁自杀死亡者的大脑中已经描述了 PDE8A mRNA 中的 RNA 编辑改变。在这里,我们研究了与年龄和性别匹配的健康对照组相比,重度抑郁症患者和自杀未遂者全血中的 PDE8A A-to-I RNA 编辑相关修饰。我们报告了在重度抑郁症患者和自杀未遂者的血液中 PDE8A 的 RNA 编辑发生了显著改变,其中自杀未遂发生在样本采集前的最后一个月内。在全血中报告的 RNA 编辑修饰与自杀死亡者大脑中观察到的变化相似。此外,不同编辑异构体的分析和组合使我们能够区分自杀未遂者和对照组。总的来说,我们的结果确定了 PDE8A 作为一个与免疫反应相关的标志物,其 RNA 编辑修饰从大脑到血液都有改变,这表明监测血液样本中 PDE8A 的 RNA 编辑修饰可能有助于评估抑郁状态和自杀风险。